510(k) K781236 ยท JSS Kit, Identification, Enterobacteriaceae
ENTEROTUBE II
| Applicant | Hoffmann-La Roche, Inc., Nutley NJ, US |
| Decision | Substantially Equivalent, Aug 31, 1978 |
| Received | Jul 20, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781236
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.